Voltammetry as a virtual potentiometric sensor in modeling of a metal-ligand system and refinement of stability constants. Part 1. Polarographic and glass electrode potentiometric study of a dynamic Cd-glycine system

A mathematical conversion of data coming from nonequilibrium and dynamic voltammetric techniques (a direct current sampled (DC) and differential pulse (DP) polarography) into potentiometric sensor type of data is described and tested on a dynamic metal-ligand system. A combined experiment involving DCP, DPP and glass electrode potentiometry (GEP) was performed on a single solution sample containing a fixed [L-T] : [M-T] ratio (acid-base titration). Dedicated potentiometric software ESTA was successfully employed in the refinement operations performed on virtual potentiometric (VP) data obtained from DC and DP polarography. It was possible to refine stability constants either separately, from VP-DC or VP-DP, or simultaneously from any combination of VP-DC, VPDP and GEP. The concept of VP-DC or VP-DP is reported for the first time and numerous documented and possible advantages are discussed. The proposed procedure can be easily utilized also by nonelectrochemists who are interested in, e.g., the ligand design strategies.